Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome-Reference-Cited by-同舟云学术

Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome

Published:2020-11-09 Issue:12 Volume:26 Page:1912-1918
ISSN:1078-8956
Container-title:Nature Medicine
language:en
Short-container-title:Nat Med

Author:

Davies Robert W.^ORCID, ,Fiksinski Ania M.^ORCID,Breetvelt Elemi J.,Williams Nigel M.,Hooper Stephen R.,Monfeuga Thomas,Bassett Anne S.^ORCID,Owen Michael J.^ORCID,Gur Raquel E.,Morrow Bernice E.,McDonald-McGinn Donna M.^ORCID,Swillen Ann^ORCID,Chow Eva W. C.,van den Bree Marianne,Emanuel Beverly S.,Vermeesch Joris R.,van Amelsvoort Therese,Arango Celso,Armando Marco,Campbell Linda E.^ORCID,Cubells Joseph F.,Eliez Stephan,Garcia-Minaur Sixto,Gothelf Doron,Kates Wendy R.,Murphy Kieran C.,Murphy Clodagh M.,Murphy Declan G.^ORCID,Philip Nicole,Repetto Gabriela M.,Shashi Vandana,Simon Tony J.,Suñer Damiàn Heine,Vicari Stefano,Scherer Stephen W.^ORCID,Bearden Carrie E.^ORCID,Vorstman Jacob A. S.^ORCID

Funder

Brain and Behavior Research Foundation

Gouvernement du Canada | Instituts de Recherche en Santé du Canada | CIHR Skin Research Training Centre

Lap-Chee Tsui Fellowship for Research Excellence

See funders listed under the NIMH International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome

U.S. Department of Health & Human Services | NIH | National Institute of Mental Health

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://www.nature.com/articles/s41591-020-1103-1.pdf